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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914606Generated: November 3, 2026

4'-Hydroxyacetophenone → HCID 28096015, compound

https://huagongshe.com/reaction/1914606

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4'-HydroxyacetophenoneHCID 7469—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 43578842HCID 43578842—
SolventMethyl Ethyl KetoneHCID 6569—
ProductHCID 28096015HCID 2809601584.4%

Reaction Steps

To a solution of 2-(2-chloroacetamido)-N-methylbenzamide 22.65 g (0.1 mol) and p-hydroxyacetophenone 16.32 g (0.12 mol) in 200 mL of butanone was added 27.60 g (0.2 mol) potassium carbonate. The mixture was stirred and heated to reflux for 4-5 hours, and monitored by TLC until the reaction was over, the reaction mixture was concentrated under reduced pressure and extracted with 300 mL of ethyl acetate to separate the organic phase, the organic phase was washed with 50 ml of 5% sodium hydroxide aqueous solution and 50 ml of brine successively, dried via anhydrous magnesium sulfate and evaporated, and the residual was purified via silica gel column chromatography to obtain 27.50 g 2-(2-(4-acetylphenoxy)acetamido)-N-methylbenzamide as white solid with yield of 84.4%, m.p. 252-253° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614214B2
Source datasetuspto-grants-2013_12
ORD IDord-4f4f053f951b47d181655c645b146c92
Source noteuspto-grants-2013_12